Canonical Allele Identifier: PA2573305637
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1362741
ClinVar RCV Id: RCV001934566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Glu133Gln
CA3530595
NM_172244.3:c.397G>C