Canonical Allele Identifier: PA2825612542
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1509525
ClinVar RCV Id: RCV002040695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ile1226Val
CA369197640
NM_001127487.2:c.3676A>G