Allele Registry

Canonical Allele Identifier: PA891865472

Gene: IVD HGNC NCBI

ClinVar Allele:

200289

ClinVar RCV:

RCV000412245

ClinVar Variation:

203792

HGVS (amino-acid)	Matching Registered Transcripts
NP_002216.3:p.Ala297Val	CA312669 NM_002225.5:c.890C>T