Canonical Allele Identifier: PA2825612559
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2933562
ClinVar RCV Id: RCV003793120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1234Ser
CA369197750
NM_001127487.2:c.3700C>T