Canonical Allele Identifier: PA2741867965
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2947433
ClinVar RCV Id: RCV003804063
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu189Asp
CA2664402304
NM_001354723.2:c.567G>T
CA2740090927
NM_001354723.2:c.567G>C