Canonical Allele Identifier: PA916057068
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 661344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu51Lys
CA351748278
NM_198156.3:c.151G>A