Allele Registry

Canonical Allele Identifier: PA341849

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020449

ClinVar Variation:

21286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Ser1602Pro	CA341848 NM_001457.4:c.4804T>C