VEGFA c.19G>C ;(p.D7H)

Variant ID: 6-43738462-G-C

NM_003376.5(VEGFA):c.19G>C;(p.D7H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic predisposition to necrotizing enterocolitis in premature infants: Current knowledge, challenges, and future directions.

Seminars In Fetal & Neonatal Medicine
Cuna, Alain A; George, Lovya L; Sampath, Venkatesh V
Publication Date: 2018-12

Variant appearance in text: VEGF: D7H
PubMed Link: 30292709
Variant Present in the following documents:
  • Main text
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