PC c.382_383delinsCT ;(p.A128L)

Variant ID: 11-66638890-GC-AG

NM_001040716.1(PC):c.382_383delinsCT;(p.A128L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition.

Hereditary Cancer In Clinical Practice
Chan, Sock Hoai SH; Chiang, Jianbang J; Ngeow, Joanne J
Publication Date: 2021-03-25

Variant appearance in text: PC: Ala128Leu
PubMed Link: 33766116
Variant Present in the following documents:
  • 13053_2021_Article_178.pdf
View BVdb publication page