Allele Registry

Canonical Allele Identifier: PA341852

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020451

ClinVar Variation:

21288

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Ala1643Ser	CA341851 NM_001457.4:c.4927G>T