Canonical Allele Identifier: PA2827722711
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229239
ClinVar RCV Id: RCV004524818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser575_Ser577delinsProGlnPro
CA2825002467
NM_001353231.2:c.1723_1729delinsCCACAGC