Canonical Allele Identifier: PA916056871
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135953
ClinVar RCV Id: RCV000123104 RCV000524493 RCV001657771 RCV002426672 RCV003460872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asp9Asn
CA020190
NM_198156.3:c.25G>A