Canonical Allele Identifier: PA916057449
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2222
ClinVar RCV Id: RCV000002308 RCV000698407 RCV002321468 RCV003407257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr112His
CA020277
NM_198156.3:c.334T>C