Allele Registry

Canonical Allele Identifier: PA2825932398

Gene: IVD HGNC NCBI

ClinVar RCV:

RCV003461762

ClinVar Variation:

2676193

HGVS (amino-acid)	Matching Registered Transcripts
NP_001152980.2:p.Met299Thr	CA391722823 NM_001159508.3:c.896T>C