Canonical Allele Identifier: PA2825190887
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 820178
ClinVar RCV Id: RCV001013381 RCV001202371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Val62Met
CA039721
NM_000551.4:c.184G>A