Canonical Allele Identifier: PA2573205665
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1433972
ClinVar RCV Id: RCV001952766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Lys181Arg
CA2573136136
NM_001354723.2:c.542A>G