Allele Registry

Canonical Allele Identifier: PA136915

Gene: WHRN HGNC NCBI

ClinVar RCV:

RCV000038891

RCV001169715

RCV001169716

RCV001204993

ClinVar Variation:

45673

HGVS (amino-acid)	Matching Registered Transcripts
NP_056219.3:p.Thr785Ile	CA136914 NM_015404.4:c.2354C>T