Allele Registry

Canonical Allele Identifier: PA2827879930

Gene: IVD HGNC NCBI

ClinVar RCV:

RCV000412119

ClinVar Variation:

371390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341526.1:p.Tyr384Cys	CA7480918 NM_001354597.3:c.1151A>G