Allele Registry

Canonical Allele Identifier: PA2826085396

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000154365

RCV000964640

ClinVar Variation:

177752

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166896.1:p.His364Arg	CA180702 NM_001173425.1:c.1091A>G