Canonical Allele Identifier: PA2825614464
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1753568
ClinVar RCV Id: RCV002361811 RCV003229087 RCV003776259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2116Ala
CA369212557
NM_001127487.2:c.6346A>G