Allele Registry

Canonical Allele Identifier: PA109097

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000590356

RCV004440400

RCV004440401

ClinVar Variation:

496052

3148494

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser80Arg	CA16621913 NM_000551.4:c.238A>C CA351750515 NM_000551.4:c.240T>G CA351750519 NM_000551.4:c.240T>A