Canonical Allele Identifier: PA2830283989
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1422865
ClinVar RCV Id: RCV001926295
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Pro39Ser
CA398535299
NM_144606.7:c.115C>T