Canonical Allele Identifier: PA916057005
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 809420
ClinVar RCV Id: RCV000997986 RCV001858871
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro40Arg
CA351747895
NM_198156.3:c.119C>G