Canonical Allele Identifier: PA2827722035
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2108099
ClinVar RCV Id: RCV003033995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser302Pro
CA398533039
NM_001353231.2:c.904T>C