Canonical Allele Identifier: PA2826913794
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16324
ClinVar RCV Id: RCV000017721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293061.2:p.Leu1793Arg
CA126366
NM_001306132.2:c.5378T>G