Allele Registry

Canonical Allele Identifier: PA107407

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011235

ClinVar Variation:

10489

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Pro160Arg	CA255271 NM_000202.8:c.479C>G