Allele Registry

Canonical Allele Identifier: PA2742030539

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003786027

ClinVar Variation:

2924277

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gly44Cys	CA351748054 NM_198156.3:c.130G>T