Canonical Allele Identifier: PA2827722605
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1775692
ClinVar RCV Id: RCV002405802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg527Pro
CA398530445
NM_001353231.2:c.1580G>C