Allele Registry

Canonical Allele Identifier: PA2825976848

Gene: FLNB HGNC NCBI

ClinVar Allele:

34139

ClinVar RCV:

RCV000020450

ClinVar Variation:

21287

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157791.1:p.Pro1603Leu	CA341850 NM_001164319.2:c.4808C>T