Canonical Allele Identifier: PA2580211455
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451838
ClinVar RCV Id: RCV003187534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Phe435Leu
CA398531742
NM_001353229.2:c.1305C>G
CA398531744
NM_001353229.2:c.1305C>A
CA398531753
NM_001353229.2:c.1303T>C