Canonical Allele Identifier: PA2825615181
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2948229
ClinVar RCV Id: RCV003807051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2531Pro
CA369219692
NM_001127487.2:c.7591A>C