Canonical Allele Identifier: PA2499252025
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1063292
ClinVar RCV Id: RCV001373116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly120Val
CA896160179
NM_001354723.2:c.359G>T