Canonical Allele Identifier: PA308796
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202090
ClinVar RCV Id: RCV000183904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Gly81del
CA308794
NM_000337.6:c.242_244del