Canonical Allele Identifier: PA2826033078
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Thr124Met
CA331784
NM_001166550.4:c.371C>T