Canonical Allele Identifier: PA206666
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Lys2232Arg
CA206665
NM_001456.4:c.6695A>G