Canonical Allele Identifier: PA115423
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2221
ClinVar RCV Id: RCV000002307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu135Phe
CA020338
NM_000551.4:c.405A>C
CA351754030
NM_000551.4:c.405A>T