Canonical Allele Identifier: PA108938
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 649525
ClinVar RCV Id: RCV000804483 RCV002336632
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro154Leu
CA351754410
NM_000551.4:c.461C>T