Canonical Allele Identifier: PA2741865197
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2624774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ile421Val
CA398531923
NM_001353229.2:c.1261A>G