Canonical Allele Identifier: PA2827719369
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2059524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala64Val
CA398535133
NM_001353229.2:c.191C>T