Canonical Allele Identifier: PA110722
Gene: IYD HGNC NCBI

Linked Data

ClinVar Variation Id: 739
ClinVar RCV Id: RCV000000775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_981932.1:p.Ile116Thr
CA114466
NM_203395.3:c.347T>C