Canonical Allele Identifier: PA2741865151
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2874015
ClinVar RCV Id: RCV003608473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser334Arg
CA398532941
NM_001353229.2:c.1002T>G
CA398532942
NM_001353229.2:c.1002T>A
CA398532947
NM_001353229.2:c.1000A>C