Canonical Allele Identifier: PA2830263890
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3010640
ClinVar RCV Id: RCV003862279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala304Thr
CA398533026
NM_144997.7:c.910G>A