Canonical Allele Identifier: PA2580228734
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2175644
ClinVar RCV Id: RCV002579386
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser146Arg
CA2580068429
NM_001354723.2:c.438C>G
CA3012357280
NM_001354723.2:c.436A>C