Canonical Allele Identifier: PA2741884731
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2937798
ClinVar RCV Id: RCV003794428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Met2167Thr
CA4476003
NM_001458.5:c.6500T>C