Canonical Allele Identifier: PA2499252022
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1017368
ClinVar RCV Id: RCV001316513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Met116Leu
CA70046659
NM_001354723.2:c.346A>T
CA1345067135
NM_001354723.2:c.346A>C