Canonical Allele Identifier: PA206667
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Lys2240Arg
CA206665
NM_001110556.2:c.6719A>G