Canonical Allele Identifier: PA2830430922
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 238112
ClinVar RCV Id: RCV000227376 RCV002354644
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln154His
CA10582118
NM_198156.3:c.462G>C
CA351756499
NM_198156.3:c.462G>T