Canonical Allele Identifier: PA2827994259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1100Arg
CA16028963
NM_001354901.2:c.3299C>G