Canonical Allele Identifier: PA302931
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 196256
ClinVar RCV Id: RCV000211553 RCV000666333 RCV000724012 RCV001043670 RCV003233485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Arg11Gln
CA302929
NM_000337.6:c.32G>A