Canonical Allele Identifier: PA2580108627
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2148543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Arg458His
CA10537450
NM_000202.8:c.1373G>A