Allele Registry

Canonical Allele Identifier: PA645438041

Gene: SGSH HGNC NCBI

ClinVar RCV:

RCV000494203

RCV000672621

RCV003235251

ClinVar Variation:

429525

HGVS (amino-acid)	Matching Registered Transcripts
NP_000190.1:p.Ser57Arg	CA401364359 NM_000199.5:c.171C>G CA401364361 NM_000199.5:c.171C>A CA401364372 NM_000199.5:c.169A>C