Canonical Allele Identifier: PA2826033336
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 10498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Arg378Gln
CA340992
NM_001166550.4:c.1133G>A