Canonical Allele Identifier: PA208449
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Val458Ile
CA208448
NM_001110556.2:c.1372G>A