Canonical Allele Identifier: PA2827721440
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Met58Thr
CA398535171
NM_001353231.2:c.173T>C