Canonical Allele Identifier: PA1139693997
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 852949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro60Leu
CA414523180
NM_001166550.4:c.179C>T