Allele Registry

Canonical Allele Identifier: PA107319

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011240

ClinVar Variation:

10494

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Lys135Arg	CA255275 NM_000202.8:c.404A>G