Canonical Allele Identifier: PA2580262675
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2185342
ClinVar RCV Id: RCV002603769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr1509Ala
CA4475367
NM_001458.5:c.4525A>G