Canonical Allele Identifier: PA1139705120
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 951944
ClinVar RCV Id: RCV001223954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2564Ile
CA369219698
NM_001458.5:c.7691C>T