Canonical Allele Identifier: PA2827980540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2473Ser
CA16037645
NM_001354899.2:c.7417G>T