Allele Registry

Canonical Allele Identifier: PA915988252

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020449

ClinVar Variation:

21286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Ser1633Pro	CA341848 NM_001164317.2:c.4897T>C