Canonical Allele Identifier: PA645469784
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 411706
ClinVar RCV Id: RCV000458794 RCV000596325 RCV002339185 RCV002489082 RCV003233644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Asp153Gly
CA3530601
NM_000337.6:c.458A>G