Canonical Allele Identifier: PA2828049067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1496036
ClinVar RCV Id: RCV003773284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Cys2538Tyr
CA16038688
NM_001354904.2:c.7613G>A