Canonical Allele Identifier: PA916035659
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 642734
ClinVar RCV Id: RCV000796248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339851.1:p.Arg233Gly
CA8817836
NM_001352922.2:c.697C>G