Canonical Allele Identifier: PA658825860
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 560745
ClinVar RCV Id: RCV000679041 RCV000698100 RCV002334238 RCV003465545 RCV004004216
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro154Arg
CA351754408
NM_000551.4:c.461C>G