Allele Registry

Canonical Allele Identifier: PA2826033337

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011243

RCV000180471

RCV000723439

ClinVar Variation:

10497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Arg378Trp	CA340991 NM_001166550.4:c.1132C>T