Allele Registry

Canonical Allele Identifier: PA107599

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011233

RCV000790725

ClinVar Variation:

10487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ser333Leu	CA340987 NM_000202.8:c.998C>T