Canonical Allele Identifier: PA645462803
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411988
ClinVar RCV Id: RCV000475786 RCV002475891 RCV004022892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg79Gly
CA16611065
NM_000551.4:c.235C>G