Canonical Allele Identifier: PA2827926766
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1462510
ClinVar RCV Id: RCV001968513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val74Leu
CA351749160
NM_001354723.2:c.220G>C