Allele Registry

Canonical Allele Identifier: PA2830430630

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002319

RCV001231697

RCV003298026

RCV004018540

ClinVar Variation:

2231

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Leu122Pro	CA020423 NM_198156.3:c.365T>C CA645525064 NM_198156.3:c.365_366delinsCT