Canonical Allele Identifier: PA356656
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 219929
ClinVar RCV Id: RCV001352159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln145Leu
CA348226
NM_000551.4:c.434A>T