Allele Registry

Canonical Allele Identifier: PA107709

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011234

ClinVar Variation:

10488

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Trp502Ser	CA255270 NM_000202.8:c.1505G>C