Allele Registry

Canonical Allele Identifier: PA1139703053

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 938780

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg1150Trp	CA4475041 NM_001458.5:c.3448C>T