Allele Registry

Canonical Allele Identifier: PA100489

Gene: FLNA HGNC NCBI

ClinVar RCV:

RCV000012523

ClinVar Variation:

11757

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104026.1:p.Asp1159Ala	CA256057 NM_001110556.2:c.3476A>C