Canonical Allele Identifier: PA2826033223
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 221201
ClinVar RCV Id: RCV000204392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Trp255Arg
CA348624
NM_001166550.4:c.763T>A
CA414518985
NM_001166550.4:c.763T>C