Canonical Allele Identifier: PA2499252052
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1024533
ClinVar RCV Id: RCV001324732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr164Ile
CA1345067421
NM_001354723.2:c.491C>T