Canonical Allele Identifier: PA323559
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ala1141Thr
CA323558
NM_001110556.2:c.3421G>A