Canonical Allele Identifier: PA2827722051
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1766403
ClinVar RCV Id: RCV002371444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Lys309Asn
CA398532983
NM_001353231.2:c.927A>C
CA398532984
NM_001353231.2:c.927A>T