Canonical Allele Identifier: PA2828029255
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Phe2337Tyr
CA16038409
NM_001354906.2:c.7010T>A