Canonical Allele Identifier: PA2825615318
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_001120959.1:p.Tyr2663Cys
CA369221683
NM_001127487.2:c.7988A>G