Allele Registry

Canonical Allele Identifier: PA1139764318

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001233308

RCV002484277

ClinVar Variation:

959877

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gly44Arg	CA351748058 NM_198156.3:c.130G>C