Canonical Allele Identifier: PA234902
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 167664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006633.1:p.Glu470Gly
CA234901
NM_006642.5:c.1409A>G