Canonical Allele Identifier: PA2741867964
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2942417
ClinVar RCV Id: RCV003805631
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu188Asp
CA2740090926
NM_001354723.2:c.564A>C