Canonical Allele Identifier: PA2499252059
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1014800
ClinVar RCV Id: RCV001313585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Lys187Arg
CA1345067554
NM_001354723.2:c.560A>G