Allele Registry

Canonical Allele Identifier: PA1139704402

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 848238

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Arg1999Trp	CA4475847 NM_001458.5:c.5995C>T