Canonical Allele Identifier: PA2828004590
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala2704Thr
CA015437
NM_001354902.2:c.8110G>A