Canonical Allele Identifier: PA221711
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 93756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Cys1108Tyr
CA221709
NM_001456.4:c.3323G>A