Canonical Allele Identifier: PA2825611200
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1513083
ClinVar RCV Id: RCV002023349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Glu637Gly
CA4474527
NM_001127487.2:c.1910A>G