Canonical Allele Identifier: PA280296
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 36903
ClinVar RCV Id: RCV000030587 RCV001022748
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu153Gln
CA020365
NM_000551.4:c.458T>A