Allele Registry

Canonical Allele Identifier: PA915988251

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020448

ClinVar Variation:

21285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Val1623Asp	CA341847 NM_001164317.2:c.4868T>A