Canonical Allele Identifier: PA2825615355
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1467621
ClinVar RCV Id: RCV001970454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro2692Arg
CA369222274
NM_001127487.2:c.8075C>G