Allele Registry

Canonical Allele Identifier: PA350642

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000206626

ClinVar Variation:

221222

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ile64Asn	CA350641 NM_000202.8:c.191T>A