Canonical Allele Identifier: PA2825666895
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1362741
ClinVar RCV Id: RCV001934566
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Glu132Gln
CA3530595
NM_001128209.2:c.394G>C