Allele Registry

Canonical Allele Identifier: PA891865482

Gene: IVD HGNC NCBI

ClinVar RCV:

RCV000412119

ClinVar Variation:

371390

HGVS (amino-acid)	Matching Registered Transcripts
NP_002216.3:p.Tyr400Cys	CA7480918 NM_002225.5:c.1199A>G