Allele Registry

Canonical Allele Identifier: PA2828171628

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000017720

ClinVar Variation:

16323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352447.1:p.Trp1834Arg	CA126364 NM_001365518.2:c.5500T>A CA350471586 NM_001365518.2:c.5500T>C