Canonical Allele Identifier: PA2826033174
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 997011
ClinVar RCV Id: RCV001564022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Ser213Phe
CA414520379
NM_001166550.4:c.638C>T