Canonical Allele Identifier: PA2741884855
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2946250
ClinVar RCV Id: RCV003806536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Tyr1230Ser
CA369197698
NM_001458.5:c.3689A>C