Canonical Allele Identifier: PA2826033345
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1186178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro383Ser
CA414518143
NM_001166550.4:c.1147C>T