Canonical Allele Identifier: PA1139704634
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 840155
ClinVar RCV Id: RCV001042078 RCV001557508 RCV002508950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2151Ser
CA369212569
NM_001458.5:c.6451G>A