Allele Registry

Canonical Allele Identifier: PA891849948

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 569381

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Pro1126Ala	CA4475027 NM_001458.5:c.3376C>G