Canonical Allele Identifier: PA1139701982
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 858685
ClinVar RCV Id: RCV001729788 RCV002374969 RCV001064615 RCV002482085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr302Met
CA4474163
NM_001458.5:c.905C>T