Allele Registry

Canonical Allele Identifier: PA107389

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000790545

ClinVar Variation:

638079

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Pro120Arg	CA414526031 NM_000202.8:c.359C>G