Canonical Allele Identifier: PA2828013072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Phe2460Tyr
CA16038409
NM_001354905.2:c.7379T>A