Allele Registry

Canonical Allele Identifier: PA319893

Gene: FLNA HGNC NCBI

ClinVar RCV:

RCV000195541

RCV001316709

ClinVar Variation:

213508

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104026.1:p.Ile1666Thr	CA319891 NM_001110556.2:c.4997T>C