Allele Registry

Canonical Allele Identifier: PA2826913642

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000207432

ClinVar Variation:

192246

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293061.2:p.Pro1381del	CA352254 NM_001306132.2:c.4142_4144del