Canonical Allele Identifier: PA2827926923
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg107His
CA357135
NM_001354723.2:c.320G>A