Canonical Allele Identifier: PA916057247
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_937799.1:p.Ser80Ile
CA16621914
NM_198156.3:c.239G>T