Canonical Allele Identifier: PA2499252030
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1044992
ClinVar RCV Id: RCV001349326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu128Phe
CA1345067205
NM_001354723.2:c.382C>T