Canonical Allele Identifier: PA322639
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Arg708Gln
CA322638
NM_001110556.2:c.2123G>A