Allele Registry

Canonical Allele Identifier: PA348965

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000204759

ClinVar Variation:

221208

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ser142Tyr	CA348964 NM_000202.8:c.425C>A