Canonical Allele Identifier: PA2827722070
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2874015
ClinVar RCV Id: RCV003608473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser316Arg
CA398532941
NM_001353231.2:c.948T>G
CA398532942
NM_001353231.2:c.948T>A
CA398532947
NM_001353231.2:c.946A>C