Canonical Allele Identifier: PA2830430581
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 958243
ClinVar RCV Id: RCV001231369 RCV002484264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu119Gln
CA351756093
NM_198156.3:c.355G>C