Canonical Allele Identifier: PA2825614084
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_001120959.1:p.Val1932Gly
CA369209052
NM_001127487.2:c.5795T>G