Allele Registry

Canonical Allele Identifier: PA096465

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020459

ClinVar Variation:

21296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Leu234Val	CA341866 NM_001457.4:c.700C>G