Canonical Allele Identifier: PA2826033334
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 638084
ClinVar RCV Id: RCV000790550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro377Leu
CA414518171
NM_001166550.4:c.1130C>T