Allele Registry

Canonical Allele Identifier: PA106675

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011243

RCV000180471

RCV000723439

ClinVar Variation:

10497

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Arg468Trp	CA340991 NM_000202.8:c.1402C>T