Canonical Allele Identifier: PA2830430885
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2119129
ClinVar RCV Id: RCV003054506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr144Phe
CA351756373
NM_198156.3:c.431A>T