Canonical Allele Identifier: PA2573205673
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1372327
ClinVar RCV Id: RCV001872900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser190Gly
CA2573136144
NM_001354723.2:c.568A>G