Canonical Allele Identifier: PA658673629
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 464023
ClinVar RCV Id: RCV000524650 RCV001152446 RCV003139765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Ala278Thr
CA3530706
NM_000337.6:c.832G>A