Allele Registry

Canonical Allele Identifier: PA2827386563

Gene: WHRN HGNC NCBI

ClinVar Allele:

54819

ClinVar RCV:

RCV000038872

RCV000888343

RCV001165873

RCV001165874

ClinVar Variation:

45654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Pro134Leu	CA136881 NM_001346890.1:c.401C>T