Allele Registry

Canonical Allele Identifier: PA100696

Gene: FLNA HGNC NCBI

ClinVar RCV:

RCV000174052

RCV000490438

RCV000755539

RCV001079269

RCV004020064

ClinVar Variation:

193845

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104026.1:p.Val528Met	CA302718 NM_001110556.2:c.1582G>A