Canonical Allele Identifier: PA177979
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 165234
ClinVar RCV Id: RCV000151873 RCV000172105 RCV000515330 RCV000700991 RCV003233117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Arg165Gln
CA177977
NM_000337.6:c.494G>A