Allele Registry

Canonical Allele Identifier: PA2827386806

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038890

RCV000278001

RCV000370224

RCV001496939

RCV001517112

ClinVar Variation:

45672

1154813

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Val432Ala	CA136912 NM_001346890.1:c.1295T>C CA2499219589 NM_001346890.1:c.1295_1296delinsCA