Canonical Allele Identifier: PA916035901
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 565465
ClinVar RCV Id: RCV000685034 RCV001010255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Val418Ala
CA8416097
NM_001353229.2:c.1253T>C