Canonical Allele Identifier: PA2828012812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala2416Thr
CA16038108
NM_001354905.2:c.7246G>A