Canonical Allele Identifier: PA100565
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Glu82Val
CA256055
NM_001110556.2:c.245A>T