Canonical Allele Identifier: PA915981061
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Pro207Leu
CA256056
NM_001456.4:c.620C>T