Canonical Allele Identifier: PA2826033381
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Val413Asp
CA220492
NM_001166550.4:c.1238T>A