Allele Registry

Canonical Allele Identifier: PA2826085795

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038881

RCV000267996

RCV000316178

RCV001517113

ClinVar Variation:

45663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166896.1:p.Met613Thr	CA136898 NM_001173425.1:c.1838T>C