Canonical Allele Identifier: PA2827720842
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1446680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg401Ser
CA398531943
NM_001353230.2:c.1201C>A