Canonical Allele Identifier: PA2828014634
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1505519
ClinVar RCV Id: RCV003773369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Glu202Gly
CA16022662
NM_001354903.2:c.605A>G