Canonical Allele Identifier: PA916057418
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg107His
CA357135
NM_198156.3:c.320G>A