Canonical Allele Identifier: PA2828048769
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Phe2494Tyr
CA16038409
NM_001354904.2:c.7481T>A