Canonical Allele Identifier: PA2830430879
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1385557
ClinVar RCV Id: RCV001905552 RCV003470996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr144Asn
CA041587
NM_198156.3:c.430T>A