Canonical Allele Identifier: PA2825611214
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1782703
ClinVar RCV Id: RCV002410736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.His641Arg
CA369227370
NM_001127487.2:c.1922A>G