Allele Registry

Canonical Allele Identifier: PA348625

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000204392

ClinVar Variation:

221201

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Trp345Arg	CA348624 NM_000202.8:c.1033T>A CA414518985 NM_000202.8:c.1033T>C