Canonical Allele Identifier: PA2573205638
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1492543
ClinVar RCV Id: RCV001981038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr145Ala
CA2573136110
NM_001354723.2:c.433A>G