Canonical Allele Identifier: PA1139734648
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 854741
ClinVar RCV Id: RCV001059851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu186Lys
CA70046819
NM_001354723.2:c.556G>A