Canonical Allele Identifier: PA2825191195
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1796579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu94Asp
CA351750796
NM_000551.4:c.282G>C
CA351750798
NM_000551.4:c.282G>T