Canonical Allele Identifier: PA2827720810
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2000398
ClinVar RCV Id: RCV002824500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Phe388Leu
CA398532134
NM_001353230.2:c.1164T>G
CA398532135
NM_001353230.2:c.1164T>A
CA398532145
NM_001353230.2:c.1162T>C