Canonical Allele Identifier: PA915984533
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 654143
ClinVar RCV Id: RCV000810039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala2041Asp
CA369211307
NM_001458.5:c.6122C>A