Canonical Allele Identifier: PA2580210191
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1973681
ClinVar RCV Id: RCV002765371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339851.1:p.Ser69Gly
CA401364214
NM_001352922.2:c.205A>G