Canonical Allele Identifier: PA658669208
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_000542.1:p.Pro97Thr
CA351750843
NM_000551.4:c.289C>A