Canonical Allele Identifier: PA916057153
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 182975
ClinVar RCV Id: RCV000626711 RCV001389259
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser65Leu
CA020104
NM_198156.3:c.194C>T