Canonical Allele Identifier: PA2573184287
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1569010
ClinVar RCV Id: RCV002218777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Val96Ala
CA10537638
NM_001166550.4:c.287T>C