Canonical Allele Identifier: PA106700
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Arg88Cys
CA220494
NM_000202.8:c.262C>T