Allele Registry

Canonical Allele Identifier: PA106666

Gene: IDS HGNC NCBI

ClinVar Allele:

25539

ClinVar RCV:

RCV000011246

ClinVar Variation:

10500

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Arg468Leu	CA121099 NM_000202.8:c.1403G>T