Canonical Allele Identifier: PA2830430567
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 182980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Leu117Pro
CA020399
NM_198156.3:c.350T>C
CA645525048
NM_198156.3:c.350_351delinsCC