Canonical Allele Identifier: PA2825666839
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1465719
ClinVar RCV Id: RCV001963789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Gly80Ala
CA362008023
NM_001128209.2:c.239G>C