Canonical Allele Identifier: PA274739
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 190194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Gln1484Arg
CA274737
NM_001456.4:c.4451A>G