Allele Registry

Canonical Allele Identifier: PA096449

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020444

RCV001379117

ClinVar Variation:

21281

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Leu1431Arg	CA341840 NM_001457.4:c.4292T>G