Canonical Allele Identifier: PA916057336
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223175
ClinVar RCV Id: RCV000208845
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly93Cys
CA357106
NM_198156.3:c.277G>T