Allele Registry

Canonical Allele Identifier: PA2825974616

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020442

ClinVar Variation:

21279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Gly363Glu	CA341837 NM_001164318.2:c.1088G>A