Canonical Allele Identifier: PA2826033231
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 996921
ClinVar RCV Id: RCV001291745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Ser259Arg
CA414518948
NM_001166550.4:c.777C>G
CA414518949
NM_001166550.4:c.777C>A
CA414518954
NM_001166550.4:c.775A>C