Allele Registry

Canonical Allele Identifier: PA2827926635

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002021926

ClinVar Variation:

1479906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly44Ala	CA351748061 NM_001354723.2:c.131G>C