Allele Registry

Canonical Allele Identifier: PA915988254

Gene: FLNB HGNC NCBI

ClinVar Allele:

34139

ClinVar RCV:

RCV000020450

ClinVar Variation:

21287

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157789.1:p.Pro1634Leu	CA341850 NM_001164317.2:c.4901C>T