Canonical Allele Identifier: PA2829630442
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1521407
ClinVar RCV Id: RCV002027870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Phe116Val
CA414526142
NM_006123.5:c.346T>G