Allele Registry

Canonical Allele Identifier: PA2829367191

Gene: IVD HGNC NCBI

ClinVar RCV:

RCV003461762

ClinVar Variation:

2676193

HGVS (amino-acid)	Matching Registered Transcripts
NP_002216.3:p.Met329Thr	CA391722823 NM_002225.5:c.986T>C