Canonical Allele Identifier: PA2826033066
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92620
ClinVar RCV Id: RCV000178730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Leu106Ser
CA220495
NM_001166550.4:c.317T>C