Canonical Allele Identifier: PA221729
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Glu254Lys
CA221728
NM_001456.4:c.760G>A