Allele Registry

Canonical Allele Identifier: PA1139725358

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV001248312

ClinVar Variation:

972313

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Val783Glu	CA374619709 NM_015404.4:c.2348T>A