Canonical Allele Identifier: PA2828019147
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727806
ClinVar RCV Id: RCV002320438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly938Val
CA16028163
NM_001354903.2:c.2813G>T