Canonical Allele Identifier: PA2580556346
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1766472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu31Gly
CA351747601
NM_198156.3:c.92A>G