Allele Registry

Canonical Allele Identifier: PA152867

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000117076

RCV000711689

RCV001510686

RCV002326814

ClinVar Variation:

129091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg1567Gln	CA152865 NM_001458.5:c.4700G>A