Allele Registry

Canonical Allele Identifier: PA2829630493

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000204759

ClinVar Variation:

221208

HGVS (amino-acid)	Matching Registered Transcripts
NP_006114.1:p.Ser142Tyr	CA348964 NM_006123.5:c.425C>A