Canonical Allele Identifier: PA2573203576
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1382962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Val330Leu
CA398532971
NM_001353229.2:c.988G>T
CA398532972
NM_001353229.2:c.988G>C