Allele Registry

Canonical Allele Identifier: PA107397

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000205759

ClinVar Variation:

221206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Pro120His	CA349872 NM_000202.8:c.359C>A