Canonical Allele Identifier: PA2830264142
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2122946
ClinVar RCV Id: RCV003054304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met370Ile
CA398532309
NM_144997.7:c.1110G>A
CA398532310
NM_144997.7:c.1110G>T
CA398532311
NM_144997.7:c.1110G>C