Canonical Allele Identifier: PA658673627
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 449229
ClinVar RCV Id: RCV000730461 RCV000695524 RCV001194184 RCV002527569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Val265Ile
CA3530698
NM_000337.6:c.793G>A