Canonical Allele Identifier: PA2830430818
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1746631
ClinVar RCV Id: RCV002344520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg136_Arg141dup
CA2580068485
NM_198156.3:c.406_423dup