Canonical Allele Identifier: PA109112
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625229
ClinVar RCV Id: RCV000767244 RCV001220559
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ser80Ile
CA16621914
NM_000551.4:c.239G>T