Canonical Allele Identifier: PA2499252034
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1010161
ClinVar RCV Id: RCV001307749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu135Val
CA1044995498
NM_001354723.2:c.403C>G