Allele Registry

Canonical Allele Identifier: PA2826086095

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038890

RCV000278001

RCV000370224

RCV001496939

RCV001517112

ClinVar Variation:

45672

1154813

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166896.1:p.Val782Ala	CA136912 NM_001173425.1:c.2345T>C CA2499219589 NM_001173425.1:c.2345_2346delinsCA