Canonical Allele Identifier: PA2828021036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1257Val
CA008903
NM_001354903.2:c.3770C>T