Canonical Allele Identifier: PA2827722177
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 950568
ClinVar RCV Id: RCV001222305 RCV003163719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro359Ser
CA8416142
NM_001353231.2:c.1075C>T