Canonical Allele Identifier: PA2828030385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala2512Thr
CA015437
NM_001354906.2:c.7534G>A