Canonical Allele Identifier: PA2573311191
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1500381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu21Lys
CA351747330
NM_198156.3:c.61G>A