Canonical Allele Identifier: PA1139739897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1776dup
CA913188211
NM_001354896.2:c.5326_5328dup