Canonical Allele Identifier: PA2573247270
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1459022
ClinVar RCV Id: RCV001949645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Ser333Trp
CA414519855
NM_006123.5:c.998C>G