Allele Registry

Canonical Allele Identifier: PA2825975382

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020451

ClinVar Variation:

21288

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Ala1643Ser	CA341851 NM_001164318.2:c.4927G>T