Canonical Allele Identifier: PA2826033219
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 946154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.His252Tyr
CA414519008
NM_001166550.4:c.754C>T