Canonical Allele Identifier: PA2828007268
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1511Thr
CA16032296
NM_001354905.2:c.4531G>A