Allele Registry

Canonical Allele Identifier: PA2826913775

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000017720

ClinVar Variation:

16323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293061.2:p.Trp1744Arg	CA126364 NM_001306132.2:c.5230T>A CA350471586 NM_001306132.2:c.5230T>C