Canonical Allele Identifier: PA308790
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_000328.2:p.Ile64Thr
CA308788
NM_000337.6:c.191T>C