APOB c.2656A>C ;(p.N886H)

Variant ID: 2-21245863-T-G

NM_000384.2(APOB):c.2656A>C;(p.N886H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic alterations associated with progression from pancreatic intraepithelial neoplasia to invasive pancreatic tumor.

Gastroenterology
Murphy, Stephen J SJ; Hart, Steven N SN; Lima, Joema Felipe JF; Kipp, Benjamin R BR; Klebig, Mitchell M; Winters, Jennifer L JL; Szabo, Csilla C; Zhang, Lizhi L; Eckloff, Bruce W BW; Petersen, Gloria M GM; Scherer, Steven E SE; Gibbs, Richard A RA; McWilliams, Robert R RR; Vasmatzis, George G; Couch, Fergus J FJ
Publication Date: 2013-11

Variant appearance in text: APOB: N886H
PubMed Link: 23912084
Variant Present in the following documents:
  • Main text
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