Canonical Allele Identifier: PA1139765176
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 864567
ClinVar RCV Id: RCV001071787
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.His110Gln
CA351751316
NM_198156.3:c.330C>A
CA351751317
NM_198156.3:c.330C>G