Canonical Allele Identifier: PA2828000856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala644Val
CA007259
NM_001354902.2:c.1931C>T