Allele Registry

Canonical Allele Identifier: PA106796

Gene: IDS HGNC NCBI

ClinVar RCV:

RCV000790544

ClinVar Variation:

638078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000193.1:p.Asn63Asp	CA337036725 NM_000202.8:c.187A>G