Canonical Allele Identifier: PA916057263
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 193118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg82Pro
CA020159
NM_198156.3:c.245G>C