Canonical Allele Identifier: PA2830264964
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 944338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala574Val
CA398529784
NM_144997.7:c.1721C>T