Canonical Allele Identifier: PA108508
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223193
ClinVar RCV Id: RCV000208843 RCV003765349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly114Arg
CA357101
NM_000551.4:c.340G>C