Canonical Allele Identifier: PA2825190734
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2952181
ClinVar RCV Id: RCV003815332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu46Asp
CA351748124
NM_000551.4:c.138G>C
CA351748127
NM_000551.4:c.138G>T