Canonical Allele Identifier: PA2825614517
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1310649
ClinVar RCV Id: RCV001767763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gln2138Arg
CA369212723
NM_001127487.2:c.6413A>G