Canonical Allele Identifier: PA2830430903
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 575315
ClinVar RCV Id: RCV000697499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asp149dup
CA891843325
NM_198156.3:c.445_447dup