Allele Registry

Canonical Allele Identifier: PA645394578

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000492930

RCV000824615

ClinVar Variation:

430477

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg1567Leu	CA369202763 NM_001458.5:c.4700G>T