Canonical Allele Identifier: PA916056914
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456586
ClinVar RCV Id: RCV000532105 RCV004023757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val13Ile
CA70042199
NM_198156.3:c.37G>A