Canonical Allele Identifier: PA916057157
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 820439
ClinVar RCV Id: RCV001013892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val66Met
CA351748808
NM_198156.3:c.196G>A