Allele Registry

Canonical Allele Identifier: PA2826086109

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038892

RCV000334982

RCV000391015

RCV001095334

RCV001514504

ClinVar Variation:

45674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166896.1:p.Asn795Lys	CA136916 NM_001173425.1:c.2385C>A CA5205652 NM_001173425.1:c.2385C>G