Allele Registry

Canonical Allele Identifier: PA1139734372

Gene: VHL HGNC NCBI

ClinVar Variation Id: 856488

ClinVar RCV Id: RCV001061961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Phe122Leu	CA70046679 NM_001354723.2:c.366C>G CA2664401562 NM_001354723.2:c.364T>C CA2664401563 NM_001354723.2:c.366C>A