Allele Registry

Canonical Allele Identifier: PA2827926633

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002006886

ClinVar Variation:

1506651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Ser43Cys	CA351748024 NM_001354723.2:c.128C>G