Canonical Allele Identifier: PA2499303363
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1052300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu17Asp
CA351747259
NM_198156.3:c.51G>C
CA351747262
NM_198156.3:c.51G>T