Canonical Allele Identifier: PA1139734479
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 864061
ClinVar RCV Id: RCV001071159
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu163Phe
CA70046796
NM_001354723.2:c.489G>C
CA2664401996
NM_001354723.2:c.489G>T