Allele Registry

Canonical Allele Identifier: PA915989930

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011247

ClinVar Variation:

10501

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Ser27del	CA255279 NM_001166550.4:c.79_81del