Canonical Allele Identifier: PA108629
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1799028
ClinVar RCV Id: RCV002435999 RCV003455513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu101Arg
CA351751004
NM_000551.4:c.302T>G