Canonical Allele Identifier: PA2827926614
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135405
ClinVar RCV Id: RCV000122259 RCV000199012 RCV000565432 RCV000662921 RCV001588971 RCV003153403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro40Leu
CA020046
NM_001354723.2:c.119C>T