Canonical Allele Identifier: PA2827991816
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala326Val
CA004066
NM_001354901.2:c.977C>T