Canonical Allele Identifier: PA100670
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ser1199Leu
CA341132
NM_001110556.2:c.3596C>T