Allele Registry

Canonical Allele Identifier: PA2825081829

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV001949645

ClinVar Variation:

1459022

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ser333Trp	CA414519855 NM_000202.8:c.998C>G