Allele Registry

Canonical Allele Identifier: PA107221

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000178730

ClinVar Variation:

92620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Leu196Ser	CA220495 NM_000202.8:c.587T>C