Canonical Allele Identifier: PA2573205672
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1402500
ClinVar RCV Id: RCV001896962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu188Gln
CA2573136143
NM_001354723.2:c.562G>C