Canonical Allele Identifier: PA106691
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 632860
ClinVar RCV Id: RCV000780348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Arg48Pro
CA414527737
NM_000202.8:c.143G>C