Canonical Allele Identifier: PA916012754
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 527322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Pro86Leu
CA414526900
NM_006123.5:c.257C>T