Canonical Allele Identifier: PA2827722033
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2451839
ClinVar RCV Id: RCV003187535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser302Ala
CA398533038
NM_001353231.2:c.904T>G