Canonical Allele Identifier: PA2828011987
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1351612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2289Gly
CA16037326
NM_001354905.2:c.6865A>G