Allele Registry

Canonical Allele Identifier: PA915989942

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000204759

ClinVar Variation:

221208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Ser52Tyr	CA348964 NM_001166550.4:c.155C>A