Canonical Allele Identifier: PA2827720012
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529978
ClinVar RCV Id: RCV001012999 RCV002499066 RCV003223660 RCV000635534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg59Cys
CA8416508
NM_001353230.2:c.175C>T