Allele Registry

Canonical Allele Identifier: PA107639

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV001912365

ClinVar Variation:

1392667

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ser71Asn	CA337036723 NM_000202.8:c.212G>A