Allele Registry

Canonical Allele Identifier: PA2825976841

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020448

ClinVar Variation:

21285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Val1592Asp	CA341847 NM_001164319.2:c.4775T>A