Canonical Allele Identifier: PA2825666894
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 177914
ClinVar RCV Id: RCV000154571 RCV000559296 RCV000671469 RCV000724393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Val131Ile
CA180989
NM_001128209.2:c.391G>A