Canonical Allele Identifier: PA2825191266
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1386064
ClinVar RCV Id: RCV001889147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro102Gln
CA351751060
NM_000551.4:c.305C>A