Allele Registry

Canonical Allele Identifier: PA106649

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011244

RCV000180473

RCV000790797

ClinVar Variation:

10498

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Arg468Gln	CA340992 NM_000202.8:c.1403G>A