Allele Registry

Canonical Allele Identifier: PA2826033377

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011234

ClinVar Variation:

10488

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Trp412Ser	CA255270 NM_001166550.4:c.1235G>C