Canonical Allele Identifier: PA2830430858
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526690
ClinVar RCV Id: RCV000631290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val140Ala
CA351756307
NM_198156.3:c.419T>C