Canonical Allele Identifier: PA916012728
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 221970
ClinVar RCV Id: RCV000207419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Asp45His
CA356953
NM_006123.5:c.133G>C