Allele Registry

Canonical Allele Identifier: PA2825975341

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020447

ClinVar Variation:

21284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Asp1583del	CA341845 NM_001164318.2:c.4747_4749del