Allele Registry

Canonical Allele Identifier: PA356489

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV003509518

ClinVar Variation:

242796

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Gly489Ala	CA356488 NM_000202.8:c.1466G>C