Allele Registry

Canonical Allele Identifier: PA343269

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV004528148

ClinVar Variation:

38960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly1612Asp	CA343268 NM_001457.4:c.4835G>A