Canonical Allele Identifier: PA2825191205
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1326284
ClinVar RCV Id: RCV001786528
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro95Arg
CA351750809
NM_000551.4:c.284C>G