Canonical Allele Identifier: PA916041596
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Phe2638Tyr
CA16038409
NM_001354896.2:c.7913T>A