Allele Registry

Canonical Allele Identifier: PA239907

Gene: WHRN HGNC NCBI

ClinVar Allele:

191257

ClinVar RCV:

RCV000174376

RCV000724279

RCV001165659

RCV001165660

ClinVar Variation:

194094

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Arg882Ser	CA239906 NM_015404.4:c.2644C>A