Canonical Allele Identifier: PA2580211371
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2122946
ClinVar RCV Id: RCV003054304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met388Ile
CA398532309
NM_001353229.2:c.1164G>A
CA398532310
NM_001353229.2:c.1164G>T
CA398532311
NM_001353229.2:c.1164G>C