Canonical Allele Identifier: PA2573164427
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1430689
ClinVar RCV Id: RCV001952503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.Asp410Gly
CA8817644
NM_000199.5:c.1229A>G