Canonical Allele Identifier: PA2830430642
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2238
ClinVar RCV Id: RCV000002326 RCV001052383 RCV001023261
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln123Arg
CA020429
NM_198156.3:c.368A>G