Allele Registry

Canonical Allele Identifier: PA2830519155

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000017720

ClinVar Variation:

16323

HGVS (amino-acid)	Matching Registered Transcripts
NP_997639.2:p.Trp1744Arg	CA126364 NM_212474.3:c.5230T>A CA350471586 NM_212474.3:c.5230T>C