Allele Registry

Canonical Allele Identifier: PA2825976963

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020455

ClinVar Variation:

21292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Gly1810Arg	CA341859 NM_001164319.2:c.5428G>A CA353354712 NM_001164319.2:c.5428G>C