Allele Registry

Canonical Allele Identifier: PA2825133238

Gene: SGCD HGNC NCBI

ClinVar RCV:

RCV000808519

RCV001785727

RCV002487741

RCV003233856

ClinVar Variation:

652862

HGVS (amino-acid)	Matching Registered Transcripts
NP_000328.2:p.Arg31Trp	CA3530486 NM_000337.6:c.91C>T