Canonical Allele Identifier: PA2827880338
Gene: IVD HGNC NCBI

Linked Data

ClinVar Variation Id: 1409489
ClinVar RCV Id: RCV001939835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341528.2:p.Ser43Arg
CA268823625
NM_001354599.3:c.129C>A
CA391743805
NM_001354599.3:c.127A>C
CA391743813
NM_001354599.3:c.129C>G