Canonical Allele Identifier: PA2499252058
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1040011
ClinVar RCV Id: RCV001343583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu182Gln
CA1345067524
NM_001354723.2:c.544G>C