Canonical Allele Identifier: PA2573205616
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499900
ClinVar RCV Id: RCV002042455
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Met116Ile
CA2573136092
NM_001354723.2:c.348G>C
CA2664401489
NM_001354723.2:c.348G>T
CA3012357169
NM_001354723.2:c.348G>A