Canonical Allele Identifier: PA2499252055
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1010269
ClinVar RCV Id: RCV001307870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg172Thr
CA1345067475
NM_001354723.2:c.515G>C