Canonical Allele Identifier: PA916057217
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 420073
ClinVar RCV Id: RCV000479941 RCV000767237 RCV001201718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ile75Ser
CA16617787
NM_198156.3:c.224T>G