Canonical Allele Identifier: PA645462983
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 238107
ClinVar RCV Id: RCV000231504 RCV000563379 RCV002500765 RCV001562617
ClinVar Variation Id: 1737542
ClinVar RCV Id: RCV002321461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Phe136Leu
CA10582115
NM_000551.4:c.408T>G
CA351754038
NM_000551.4:c.406T>C
CA351754052
NM_000551.4:c.408T>A