Allele Registry

Canonical Allele Identifier: PA2825976025

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020456

ClinVar Variation:

21293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Ala201Val	CA341860 NM_001164319.2:c.602C>T