Allele Registry

Canonical Allele Identifier: PA916029078

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038866

RCV001168063

RCV001168064

RCV001206517

ClinVar Variation:

45648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Arg99His	CA136870 NM_001346890.1:c.296G>A