Allele Registry

Canonical Allele Identifier: PA096395

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000030663

RCV001064985

ClinVar Variation:

6406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly1691Ser	CA130019 NM_001457.4:c.5071G>A