Canonical Allele Identifier: PA2830430871
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411985
ClinVar RCV Id: RCV000476376 RCV001007624 RCV002349982 RCV003237874 RCV004001991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser142Leu
CA041537
NM_198156.3:c.425C>T