Canonical Allele Identifier: PA2827719959
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451832
ClinVar RCV Id: RCV003187528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Asp37Glu
CA398535308
NM_001353230.2:c.111C>G
CA398535309
NM_001353230.2:c.111C>A