Allele Registry

Canonical Allele Identifier: PA2828170886

Gene: FN1 HGNC NCBI

ClinVar Allele:

31364

ClinVar RCV:

RCV000017722

RCV002482881

ClinVar Variation:

16325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352447.1:p.Tyr973Cys	CA126368 NM_001365518.2:c.2918A>G