Canonical Allele Identifier: PA107514
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1509031
ClinVar RCV Id: RCV002040570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Pro480Leu
CA414518089
NM_000202.8:c.1439C>T