Canonical Allele Identifier: PA2830430926
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1750054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln154Arg
CA351756496
NM_198156.3:c.461A>G