Allele Registry

Canonical Allele Identifier: PA916035659

Gene: SGSH HGNC NCBI

ClinVar RCV:

RCV000796248

ClinVar Variation:

642734

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