Canonical Allele Identifier: PA324963
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.His1443Asn
CA324962
NM_001110556.2:c.4327C>A