Canonical Allele Identifier: PA2741865193
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro414His
CA398531989
NM_001353229.2:c.1241C>A