Allele Registry

Canonical Allele Identifier: PA915988338

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000362857

RCV001753815

RCV004021926

ClinVar Variation:

346367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Ala2543Thr	CA2469716 NM_001164317.2:c.7627G>A