Allele Registry

Canonical Allele Identifier: PA220491

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000180472

RCV004526612

ClinVar Variation:

92615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Arg468Pro	CA220490 NM_000202.8:c.1403G>C