Canonical Allele Identifier: PA2825615352
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1034866
ClinVar RCV Id: RCV001337650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val2691Ala
CA4476439
NM_001127487.2:c.8072T>C