Canonical Allele Identifier: PA2573205670
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1428633
ClinVar RCV Id: RCV001936407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro185Arg
CA540875888
NM_001354723.2:c.554C>G