Canonical Allele Identifier: PA1139734751
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 851353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu189Lys
CA70046821
NM_001354723.2:c.565G>A