Canonical Allele Identifier: PA2825611119
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2123767
ClinVar RCV Id: RCV003055244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu604Pro
CA369227116
NM_001127487.2:c.1811T>C