Canonical Allele Identifier: PA2825666912
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 411706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Asp152Gly
CA3530601
NM_001128209.2:c.455A>G