Canonical Allele Identifier: PA2580228752
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2006289
ClinVar RCV Id: RCV002837681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg157Ser
CA2580068439
NM_001354723.2:c.469C>A