Canonical Allele Identifier: PA2828054359
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala575Val
CA007259
NM_001354905.2:c.1724C>T