Canonical Allele Identifier: PA916057347
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2237
ClinVar RCV Id: RCV000002325 RCV000208813 RCV000698471 RCV002433441 RCV003460405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly93Ser
CA020230
NM_198156.3:c.277G>A