Allele Registry

Canonical Allele Identifier: PA2827386805

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV001248312

ClinVar Variation:

972313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Val432Glu	CA374619709 NM_001346890.1:c.1295T>A