Allele Registry

Canonical Allele Identifier: PA180703

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000154365

RCV000964640

ClinVar Variation:

177752

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.His364Arg	CA180702 NM_015404.4:c.1091A>G