Canonical Allele Identifier: PA109280
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2224
ClinVar RCV Id: RCV000002310 RCV000220823 RCV001851578 RCV002288459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Val166Phe
CA020436
NM_000551.4:c.496G>T