Canonical Allele Identifier: PA916056915
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val13Gly
CA351747163
NM_198156.3:c.38T>G