Canonical Allele Identifier: PA2827926438
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 182981
ClinVar RCV Id: RCV000161089 RCV000168429 RCV000294881 RCV000492422 RCV000781920 RCV003416030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro2Leu
CA020518
NM_001354723.2:c.5C>T