Canonical Allele Identifier: PA221713
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 93757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Val1127Met
CA221712
NM_001110556.2:c.3379G>A