Canonical Allele Identifier: PA916035854
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 579661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro329Leu
CA398532974
NM_001353229.2:c.986C>T