Allele Registry

Canonical Allele Identifier: PA2825610890

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 1773787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120959.1:p.Phe497Leu	CA369225698 NM_001127487.2:c.1489T>C CA369225708 NM_001127487.2:c.1491C>A CA369225710 NM_001127487.2:c.1491C>G