Canonical Allele Identifier: PA2741867957
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2947387
ClinVar RCV Id: RCV003801577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val124Glu
CA2740090914
NM_001354723.2:c.371T>A