Allele Registry

Canonical Allele Identifier: PA2826086094

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV001248312

ClinVar Variation:

972313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166896.1:p.Val782Glu	CA374619709 NM_001173425.1:c.2345T>A