Allele Registry

Canonical Allele Identifier: PA2825515447

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV001248312

ClinVar Variation:

972313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001077354.2:p.Val400Glu	CA374619709 NM_001083885.3:c.1199T>A