Canonical Allele Identifier: PA2827926609
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 818440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly39Ser
CA351747863
NM_001354723.2:c.115G>A