PAH c.1065+7C>A

Variant ID: 12-103238107-G-T

NM_000277.1(PAH):c.1065+7C>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Evaluation of Bioinformatic Programmes for the Analysis of Variants within Splice Site Consensus Regions.

Advances In Bioinformatics
Tang, Rongying R; Prosser, Debra O DO; Love, Donald R DR
Publication Date: 2016

Variant appearance in text: PAH: 1065+7C>A
PubMed Link: 27313609
Variant Present in the following documents:
  • 5614058.f1.pdf
View BVdb publication page