Canonical Allele Identifier: PA100475
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Arg196Trp
CA234009
NM_001110556.2:c.586C>T