Allele Registry

Canonical Allele Identifier: PA350786

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000206790

RCV001092169

ClinVar Variation:

221205

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Ser61Pro	CA350785 NM_000202.8:c.181T>C