Canonical Allele Identifier: PA915980957
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11767
ClinVar RCV Id: RCV000012533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ala128Val
CA256061
NM_001456.4:c.383C>T