Canonical Allele Identifier: PA2825615186
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2954187
ClinVar RCV Id: RCV003813410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Met2533Val
CA369219713
NM_001127487.2:c.7597A>G