Canonical Allele Identifier: PA645382000
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 286847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ala334Thr
CA10605588
NM_001456.4:c.1000G>A