Allele Registry

Canonical Allele Identifier: PA136871

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038866

RCV001168063

RCV001168064

RCV001206517

ClinVar Variation:

45648

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Arg450His	CA136870 NM_015404.4:c.1349G>A