Canonical Allele Identifier: PA2573301147
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1422865
ClinVar RCV Id: RCV001926295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro39Ser
CA398535299
NM_144997.7:c.115C>T