Canonical Allele Identifier: PA2580262617
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1734241
ClinVar RCV Id: RCV002349042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1239Leu
CA369197819
NM_001458.5:c.3716C>T