Canonical Allele Identifier: PA2825190479
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1382528
ClinVar RCV Id: RCV001890358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala11Ser
CA351747111
NM_000551.4:c.31G>T