Canonical Allele Identifier: PA108279
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2566466
ClinVar RCV Id: RCV003306573
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg79Pro
CA351749311
NM_000551.4:c.236G>C
CA645524748
NM_000551.4:c.236_237delinsCA