Allele Registry

Canonical Allele Identifier: PA658673625

Gene: SGCD HGNC NCBI

ClinVar RCV:

RCV000526167

RCV001170140

RCV003482280

ClinVar Variation:

464021

HGVS (amino-acid)	Matching Registered Transcripts
NP_000328.2:p.Thr256Met	CA3530692 NM_000337.6:c.767C>T