Canonical Allele Identifier: PA2580211255
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451839
ClinVar RCV Id: RCV003187535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser320Ala
CA398533038
NM_001353229.2:c.958T>G