Canonical Allele Identifier: PA2580211329
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2066171
ClinVar RCV Id: RCV002948954 RCV003308368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala376Ser
CA398532389
NM_001353229.2:c.1126G>T