Canonical Allele Identifier: PA915984469
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 665267
ClinVar RCV Id: RCV000823509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1965Gly
CA369209052
NM_001458.5:c.5894T>G