Canonical Allele Identifier: PA2825191047
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 821314
ClinVar RCV Id: RCV001015609 RCV001219698
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg82His
CA351750549
NM_000551.4:c.245G>A