Canonical Allele Identifier: PA2828028149
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1351612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2166Gly
CA16037326
NM_001354906.2:c.6496A>G