Allele Registry

Canonical Allele Identifier: PA658802839

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000598044

ClinVar Variation:

501150

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Pro160His	CA414523038 NM_000202.8:c.479C>A