Canonical Allele Identifier: PA2825133327
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2154170
ClinVar RCV Id: RCV003069143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Ala91Thr
CA130613351
NM_000337.6:c.271G>A