Canonical Allele Identifier: PA916057210
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625223
ClinVar RCV Id: RCV000767236 RCV001855961
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val74Asp
CA351749169
NM_198156.3:c.221T>A
CA645524719
NM_198156.3:c.221_222delinsAT