Canonical Allele Identifier: PA108295
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 193118
ClinVar RCV Id: RCV000173161 RCV000724457
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg82Pro
CA020159
NM_000551.4:c.245G>C