Allele Registry

Canonical Allele Identifier: PA891849857

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000685417

ClinVar Variation:

565776

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg650Gly	CA4474538 NM_001458.5:c.1948C>G