Canonical Allele Identifier: PA2499252026
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1035413
ClinVar RCV Id: RCV001338277
ClinVar Variation Id: 1059088
ClinVar RCV Id: RCV001368308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val124Leu
CA1345067182
NM_001354723.2:c.370G>C
CA2499216360
NM_001354723.2:c.370G>T