Canonical Allele Identifier: PA2825081487
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 642353
ClinVar RCV Id: RCV000795807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Val111Leu
CA414526249
NM_000202.8:c.331G>T
CA414526253
NM_000202.8:c.331G>C