Canonical Allele Identifier: PA2828012119
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2308Ala
CA047997
NM_001354905.2:c.6922T>G