Allele Registry

Canonical Allele Identifier: PA2830430869

Gene: VHL HGNC NCBI

ClinVar Allele:

217071

ClinVar RCV:

RCV000203537

RCV001853277

ClinVar Variation:

219158

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ser142Trp	CA277912 NM_198156.3:c.425C>G