Allele Registry

Canonical Allele Identifier: PA2827926639

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003786027

ClinVar Variation:

2924277

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly44Cys	CA351748054 NM_001354723.2:c.130G>T