Canonical Allele Identifier: PA658669249
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 486710
ClinVar RCV Id: RCV000568082 RCV000707457 RCV003441963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu129Val
CA040734
NM_000551.4:c.385C>G