Allele Registry

Canonical Allele Identifier: PA2827926808

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001379600

ClinVar Variation:

1068142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Pro81Ala	CA351750524 NM_001354723.2:c.241C>G