Canonical Allele Identifier: PA2499252047
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1014016
ClinVar RCV Id: RCV001312692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg160Leu
CA1345067402
NM_001354723.2:c.479G>T