Allele Registry

Canonical Allele Identifier: PA2825613416

Gene: FLNC HGNC NCBI

ClinVar Variation Id: 472079

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120959.1:p.Thr1597Met	CA4475458 NM_001127487.2:c.4790C>T