Canonical Allele Identifier: PA916057000
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 648840
ClinVar RCV Id: RCV000803648 RCV002453779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser38Phe
CA351747838
NM_198156.3:c.113C>T