Allele Registry

Canonical Allele Identifier: PA1139702980

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 860132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Glu1104Lys	CA4475015 NM_001458.5:c.3310G>A