Allele Registry

Canonical Allele Identifier: PA2827879852

Gene: IVD HGNC NCBI

ClinVar Allele:

200289

ClinVar RCV:

RCV000412245

ClinVar Variation:

203792

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341526.1:p.Ala281Val	CA312669 NM_001354597.3:c.842C>T