Canonical Allele Identifier: PA1139737343
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 857899
ClinVar RCV Id: RCV001063666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu331Val
CA398532966
NM_001353229.2:c.991T>G