Allele Registry

Canonical Allele Identifier: PA891850086

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 567868

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg2045Gln	CA4475896 NM_001458.5:c.6134G>A