Canonical Allele Identifier: PA2499252054
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1062475
ClinVar RCV Id: RCV001372197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp171Arg
CA2499216367
NM_001354723.2:c.511T>C
CA2664402086
NM_001354723.2:c.511T>A