Allele Registry

Canonical Allele Identifier: PA2825974612

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020441

ClinVar Variation:

21278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Gly361Ser	CA341836 NM_001164318.2:c.1081G>A