Allele Registry

Canonical Allele Identifier: PA106945

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011239

ClinVar Variation:

10493

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Cys422Gly	CA255274 NM_000202.8:c.1264T>G