Canonical Allele Identifier: PA2827926539
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1403440
ClinVar RCV Id: RCV001898786 RCV002361206 RCV004010826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu22Gly
CA351747380
NM_001354723.2:c.65A>G