Canonical Allele Identifier: PA2830430803
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 825586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr134Phe
CA351756230
NM_198156.3:c.401A>T