Canonical Allele Identifier: PA2828028372
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1449206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln2197Glu
CA16037517
NM_001354906.2:c.6589C>G