Allele Registry

Canonical Allele Identifier: PA2827926952

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001295407

ClinVar Variation:

999410

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Arg113Gly	CA351751365 NM_001354723.2:c.337C>G