Canonical Allele Identifier: PA2741865334
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2915148
ClinVar RCV Id: RCV003607133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Tyr579Cys
CA398529862
NM_001353229.2:c.1736A>G