Allele Registry

Canonical Allele Identifier: PA096413

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020441

ClinVar Variation:

21278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly361Ser	CA341836 NM_001457.4:c.1081G>A