Canonical Allele Identifier: PA2830430701
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2219
ClinVar RCV Id: RCV000002304 RCV000466046 RCV002336073
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg126Gly
CA020446
NM_198156.3:c.376C>G