Allele Registry

Canonical Allele Identifier: PA106700

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000177014

RCV000790676

ClinVar Variation:

92618

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Arg88Cys	CA220494 NM_000202.8:c.262C>T