Allele Registry

Canonical Allele Identifier: PA658678588

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000558786

ClinVar Variation:

472089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Ser1728Gly	CA369204368 NM_001458.5:c.5182A>G