Allele Registry

Canonical Allele Identifier: PA2825614670

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 2143831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120959.1:p.Phe2192Leu	CA369213094 NM_001127487.2:c.6574T>C CA369213104 NM_001127487.2:c.6576C>A CA369213106 NM_001127487.2:c.6576C>G