Allele Registry

Canonical Allele Identifier: PA106935

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000790549

ClinVar Variation:

638083

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Cys422Arg	CA414518469 NM_000202.8:c.1264T>C