Canonical Allele Identifier: PA2830430555
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2203307
ClinVar RCV Id: RCV002651640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val114Gly
CA16621938
NM_198156.3:c.341T>G
CA645525031
NM_198156.3:c.341_342delinsGC