Allele Registry

Canonical Allele Identifier: PA2827386816

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038892

RCV000334982

RCV000391015

RCV001095334

RCV001514504

ClinVar Variation:

45674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Asn445Lys	CA136916 NM_001346890.1:c.1335C>A CA5205652 NM_001346890.1:c.1335C>G