Allele Registry

Canonical Allele Identifier: PA2827881239

Gene: IVD HGNC NCBI

ClinVar RCV:

RCV000174064

RCV003330425

ClinVar Variation:

94051

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341530.2:p.Cys378Arg	CA221931 NM_001354601.3:c.1132T>C