Canonical Allele Identifier: PA2499303390
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1057750
ClinVar RCV Id: RCV001366797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Thr105Met
CA040253
NM_198156.3:c.314C>T