Allele Registry

Canonical Allele Identifier: PA915988275

Gene: FLNB HGNC NCBI

ClinVar RCV:

RCV000020455

ClinVar Variation:

21292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Gly1865Arg	CA341859 NM_001164317.2:c.5593G>A CA353354712 NM_001164317.2:c.5593G>C