Canonical Allele Identifier: PA322916
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Val1863Ile
CA322914
NM_001110556.2:c.5587G>A