Canonical Allele Identifier: PA645426565
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro326Ser
CA8416183
NM_144997.7:c.976C>T