Canonical Allele Identifier: PA132477
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 43358
ClinVar RCV Id: RCV000036266 RCV000172107 RCV000365095 RCV000404763 RCV000584814 RCV001084187 RCV001293129 RCV003944896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Gln283Arg
CA132475
NM_000337.6:c.848A>G