Canonical Allele Identifier: PA109171
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2228
ClinVar RCV Id: RCV000002316
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Tyr112Asn
CA020273
NM_000551.4:c.334T>A