Canonical Allele Identifier: PA357035
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223183
ClinVar RCV Id: RCV000208803 RCV000679030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly104Val
CA357033
NM_000551.4:c.311G>T