Allele Registry

Canonical Allele Identifier: PA2825975216

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000425923

ClinVar Variation:

392384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Ala1356Thr	CA2468652 NM_001164318.2:c.4066G>A