Canonical Allele Identifier: PA916057388
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 219160
ClinVar RCV Id: RCV000203508 RCV000208847 RCV001064921 RCV002433899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr98Ser
CA279916
NM_198156.3:c.293A>C