Allele Registry

Canonical Allele Identifier: PA2826033206

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000011233

RCV000790725

ClinVar Variation:

10487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160022.1:p.Ser243Leu	CA340987 NM_001166550.4:c.728C>T