Canonical Allele Identifier: PA109183
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2222
ClinVar RCV Id: RCV000002308 RCV000698407 RCV002321468 RCV003407257
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Tyr112His
CA020277
NM_000551.4:c.334T>C