Allele Registry

Canonical Allele Identifier: PA096431

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020442

ClinVar Variation:

21279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly363Glu	CA341837 NM_001457.4:c.1088G>A