Canonical Allele Identifier: PA2826033242
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1126548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Tyr272Cys
CA10537503
NM_001166550.4:c.815A>G