Canonical Allele Identifier: PA2825666948
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 411709
ClinVar RCV Id: RCV000457156 RCV000732478 RCV002475887 RCV003168854 RCV003233646 RCV003488618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Lys188Arg
CA3530627
NM_001128209.2:c.563A>G