Canonical Allele Identifier: PA2826033206
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 10487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Ser243Leu
CA340987
NM_001166550.4:c.728C>T