Canonical Allele Identifier: PA658682635
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 452477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Gly1457Ser
CA337279301
NM_001456.4:c.4369G>A