Canonical Allele Identifier: PA2827721163
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 937060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Thr522Ser
CA398530476
NM_001353230.2:c.1565C>G
CA398530479
NM_001353230.2:c.1564A>T