Allele Registry

Canonical Allele Identifier: PA2825975480

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020455

ClinVar Variation:

21292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Gly1823Arg	CA341859 NM_001164318.2:c.5467G>A CA353354712 NM_001164318.2:c.5467G>C