Allele Registry

Canonical Allele Identifier: PA915988259

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV004528148

ClinVar Variation:

38960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly1643Asp	CA343268 NM_001164317.2:c.4928G>A