Canonical Allele Identifier: PA2827720672
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 835557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser329Phe
CA8416179
NM_001353230.2:c.986C>T