Canonical Allele Identifier: PA1139734620
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 857169
ClinVar RCV Id: RCV001062788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro185Ala
CA896160299
NM_001354723.2:c.553C>G