Canonical Allele Identifier: PA2828028510
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala2218Ser
CA16037645
NM_001354906.2:c.6652G>T