Canonical Allele Identifier: PA915960429
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 825946
ClinVar RCV Id: RCV001024492 RCV001294333
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro192Arg
CA70052552
NM_000551.4:c.575C>G