Allele Registry

Canonical Allele Identifier: PA2827880582

Gene: IVD HGNC NCBI

ClinVar Allele:

200289

ClinVar RCV:

RCV000412245

ClinVar Variation:

203792

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341528.2:p.Ala326Val	CA312669 NM_001354599.3:c.977C>T