Canonical Allele Identifier: PA2827722313
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 574519
ClinVar RCV Id: RCV000696473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Cys415Arg
CA398531776
NM_001353231.2:c.1243T>C