Canonical Allele Identifier: PA2825610436
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2065671
ClinVar RCV Id: RCV002958646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala266Thr
CA369222484
NM_001127487.2:c.796G>A