Canonical Allele Identifier: PA2827926648
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2952181
ClinVar RCV Id: RCV003815332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu46Asp
CA351748124
NM_001354723.2:c.138G>C
CA351748127
NM_001354723.2:c.138G>T