Allele Registry

Canonical Allele Identifier: PA341842

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020445

ClinVar Variation:

21282

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Trp148Arg	CA341841 NM_001457.4:c.442T>A CA353333430 NM_001457.4:c.442T>C