Canonical Allele Identifier: PA2825614462
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2928789
ClinVar RCV Id: RCV003789563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala2115Thr
CA369212551
NM_001127487.2:c.6343G>A