Canonical Allele Identifier: PA221698
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 93749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Gln45Arg
CA221696
NM_001456.4:c.134A>G