Canonical Allele Identifier: PA915989930
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 10501
ClinVar RCV Id: RCV000011247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Ser27del
CA255279
NM_001166550.4:c.79_81del