Canonical Allele Identifier: PA2580262804
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1753568
ClinVar RCV Id: RCV002361811 RCV003229087 RCV003776259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2149Ala
CA369212557
NM_001458.5:c.6445A>G