Canonical Allele Identifier: PA220493
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Val503Asp
CA220492
NM_000202.8:c.1508T>A