Canonical Allele Identifier: PA1139765078
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 963709
ClinVar RCV Id: RCV001237774 RCV003332312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val83Leu
CA040005
NM_198156.3:c.247G>C