Canonical Allele Identifier: PA2828007497
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Tyr940Cys
CA16028105
NM_001354902.2:c.2819A>G