Canonical Allele Identifier: PA2573203232
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1514303
ClinVar RCV Id: RCV002029222 RCV004046804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339851.1:p.Val243Ile
CA8817824
NM_001352922.2:c.727G>A