Allele Registry

Canonical Allele Identifier: PA269450

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000114316

ClinVar Variation:

126375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Ala173Thr	CA269449 NM_001457.4:c.517G>A