Canonical Allele Identifier: PA2825614511
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_001120959.1:p.Met2134Thr
CA4476003
NM_001127487.2:c.6401T>C