Allele Registry

Canonical Allele Identifier: PA658808696

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000649128

ClinVar Variation:

539398

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Thr396Ala	CA369224283 NM_001458.5:c.1186A>G