Allele Registry

Canonical Allele Identifier: PA2825191364

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001295407

ClinVar Variation:

999410

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg113Gly	CA351751365 NM_000551.4:c.337C>G