Canonical Allele Identifier: PA2741884783
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_001449.3:p.Thr2564Pro
CA369219692
NM_001458.5:c.7690A>C