Allele Registry

Canonical Allele Identifier: PA106839

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000489884

RCV001376700

RCV002420251

ClinVar Variation:

427181

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Asp269Val	CA414521897 NM_000202.8:c.806A>T