Canonical Allele Identifier: PA2573205634
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1523045
ClinVar RCV Id: RCV002048815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr143Ile
CA896160255
NM_001354723.2:c.428C>T