Allele Registry

Canonical Allele Identifier: PA096552

Gene: FLNC HGNC NCBI

ClinVar RCV:

RCV000022428

RCV001781296

ClinVar Variation:

29591

HGVS (amino-acid)	Matching Registered Transcripts
NP_001449.3:p.Met251Thr	CA128477 NM_001458.5:c.752T>C