Canonical Allele Identifier: PA2828028650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala2400Ser
CA16037645
NM_001354903.2:c.7198G>T