Canonical Allele Identifier: PA2825191217
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 3232219
ClinVar RCV Id: RCV004520902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro97Arg
CA351750869
NM_000551.4:c.290C>G