Canonical Allele Identifier: PA2580211610
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2091921
ClinVar RCV Id: RCV003015851 RCV003308420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro546Ser
CA398530441
NM_001353229.2:c.1636C>T