Allele Registry

Canonical Allele Identifier: PA136913

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038890

RCV000278001

RCV000370224

RCV001496939

RCV001517112

ClinVar Variation:

45672

1154813

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Val783Ala	CA136912 NM_015404.4:c.2348T>C CA2499219589 NM_015404.4:c.2348_2349delinsCA