Canonical Allele Identifier: PA2826033253
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1302719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Gly284Val
CA414518789
NM_001166550.4:c.851G>T