Allele Registry

Canonical Allele Identifier: PA2827386665

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038881

RCV000267996

RCV000316178

RCV001517113

ClinVar Variation:

45663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333819.1:p.Met262Thr	CA136898 NM_001346890.1:c.785T>C