Allele Registry

Canonical Allele Identifier: PA115423

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002307

ClinVar Variation:

2221

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu135Phe	CA020338 NM_000551.4:c.405A>C CA351754030 NM_000551.4:c.405A>T