Canonical Allele Identifier: PA108766
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 419447
ClinVar RCV Id: RCV000484822 RCV001258069
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu184Pro
CA16617792
NM_000551.4:c.551T>C