Canonical Allele Identifier: PA658673606
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 464019
ClinVar RCV Id: RCV000537732 RCV002506334 RCV003233706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Ser145Cys
CA362010491
NM_000337.6:c.434C>G