Allele Registry

Canonical Allele Identifier: PA2825973478

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020453

ClinVar Variation:

21290

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly181Val	CA341855 NM_001164317.2:c.542G>T