Canonical Allele Identifier: PA2580117576
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1740140
ClinVar RCV Id: RCV002333559 RCV003094668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro146Arg
CA351754250
NM_000551.4:c.437C>G