Canonical Allele Identifier: PA2580228839
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2078497
ClinVar RCV Id: RCV002993803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu188Ala
CA2580068451
NM_001354723.2:c.563A>C