Canonical Allele Identifier: PA645438058
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 325838
ClinVar RCV Id: RCV000296141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.Tyr240Asn
CA10640907
NM_000199.5:c.718T>A