Canonical Allele Identifier: PA2827720773
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1794179
ClinVar RCV Id: RCV002428629
ClinVar Variation Id: 1794202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met370Leu
CA398532314
NM_001353230.2:c.1108A>T
CA398532316
NM_001353230.2:c.1108A>C