Canonical Allele Identifier: PA2827926849
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411978
ClinVar RCV Id: RCV000464337 RCV001016453
ClinVar Variation Id: 821712
ClinVar RCV Id: RCV001016401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Phe91Leu
CA16611270
NM_001354723.2:c.273C>A
CA351750722
NM_001354723.2:c.271T>C
CA351750747
NM_001354723.2:c.273C>G