Canonical Allele Identifier: PA2827720609
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 944784
ClinVar RCV Id: RCV001215263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala304Val
CA398533022
NM_001353230.2:c.911C>T