Canonical Allele Identifier: PA2828012544
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2371Ala
CA16037824
NM_001354905.2:c.7111T>G