Canonical Allele Identifier: PA2828028276
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2185Ala
CA047997
NM_001354906.2:c.6553T>G