Canonical Allele Identifier: PA916057373
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456579
ClinVar RCV Id: RCV000536081
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro97Thr
CA351750843
NM_198156.3:c.289C>A