Canonical Allele Identifier: PA916056890
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 374982
ClinVar RCV Id: RCV000476548 RCV001016912 RCV000415643 RCV001584111 RCV002488864 RCV003463824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu10Lys
CA16043991
NM_198156.3:c.28G>A