Canonical Allele Identifier: PA2828011401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys2197Glu
CA16036732
NM_001354905.2:c.6589A>G