Canonical Allele Identifier: PA2828009497
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly1898Asp
CA010991
NM_001354905.2:c.5693G>A