Allele Registry

Canonical Allele Identifier: PA341856

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020453

ClinVar Variation:

21290

HGVS (amino-acid)	Matching Registered Transcripts
NP_001448.2:p.Gly181Val	CA341855 NM_001457.4:c.542G>T