Canonical Allele Identifier: PA2825612341
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 569381
ClinVar RCV Id: RCV000689993 RCV002458223 RCV003150331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1126Ala
CA4475027
NM_001127487.2:c.3376C>G