Canonical Allele Identifier: PA2825666905
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_001121681.1:p.Ser144Cys
CA362010491
NM_001128209.2:c.431C>G