Canonical Allele Identifier: PA645382041
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 423675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Thr408Met
CA10561236
NM_001456.4:c.1223C>T