Allele Registry

Canonical Allele Identifier: PA915988282

Gene: FLNB HGNC NCBI

ClinVar Variation Id: 346353

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Glu2004Lys	CA2469211 NM_001164317.2:c.6010G>A