Allele Registry

Canonical Allele Identifier: PA2825975358

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020450

ClinVar Variation:

21287

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157790.1:p.Pro1603Leu	CA341850 NM_001164318.2:c.4808C>T