Canonical Allele Identifier: PA2826033398
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2047467
ClinVar RCV Id: RCV002904325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Asn447Ser
CA414517698
NM_001166550.4:c.1340A>G