Canonical Allele Identifier: PA2825666824
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202088
ClinVar RCV Id: RCV000183902 RCV000705812 RCV002408816 RCV002500550 RCV003233490 RCV003317134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Ile63Thr
CA308788
NM_001128209.2:c.188T>C