Canonical Allele Identifier: PA2573217910
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1413290
ClinVar RCV Id: RCV001925829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Tyr2696Cys
CA369221683
NM_001458.5:c.8087A>G