Canonical Allele Identifier: PA916056976
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 418538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly30Glu
CA16617781
NM_198156.3:c.89G>A