Allele Registry

Canonical Allele Identifier: PA2825081709

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV002029670

ClinVar Variation:

1514942

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Asp269Gly	CA414521898 NM_000202.8:c.806A>G