Allele Registry

Canonical Allele Identifier: PA100585

Gene: FLNA HGNC NCBI

ClinVar Allele:

26816

ClinVar RCV:

RCV000012544

ClinVar Variation:

11777

HGVS (amino-acid)	Matching Registered Transcripts
NP_001104026.1:p.Gly288Arg	CA121667 NM_001110556.2:c.862G>A CA415248280 NM_001110556.2:c.862G>C