Canonical Allele Identifier: PA2825190482
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 937122
ClinVar RCV Id: RCV001206074 RCV001586049 RCV003469335 RCV004033664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu12Leu
CA1139655721
NM_000551.4:c.34_35delinsTT