Canonical Allele Identifier: PA913192853
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 624448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ser149Ala
CA10537658
NM_000202.8:c.445T>G