Canonical Allele Identifier: PA2499252039
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1057078
ClinVar RCV Id: RCV001365997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gln147Arg
CA896160258
NM_001354723.2:c.440A>G