Allele Registry

Canonical Allele Identifier: PA184258

Gene: WHRN HGNC NCBI

ClinVar Allele:

174684

ClinVar RCV:

RCV000156142

RCV001168958

RCV001168959

RCV001422011

ClinVar Variation:

179353

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Gly7Arg	CA184257 NM_015404.4:c.19G>C