Allele Registry

Canonical Allele Identifier: PA915989953

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011235

ClinVar Variation:

10489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Pro70Arg	CA255271 NM_001166550.4:c.209C>G