Canonical Allele Identifier: PA2828028851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2272Ala
CA16037981
NM_001354906.2:c.6814T>G