Canonical Allele Identifier: PA2827720774
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2122946
ClinVar RCV Id: RCV003054304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met370Ile
CA398532309
NM_001353230.2:c.1110G>A
CA398532310
NM_001353230.2:c.1110G>T
CA398532311
NM_001353230.2:c.1110G>C