Canonical Allele Identifier: PA302928
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 196255
ClinVar RCV Id: RCV000212998 RCV000554394 RCV000723938 RCV000852562 RCV001156233 RCV002485153 RCV003233484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Arg31Gln
CA302926
NM_000337.6:c.92G>A