Allele Registry

Canonical Allele Identifier: PA2826912028

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000207432

ClinVar Variation:

192246

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293059.2:p.Pro1472del	CA352254 NM_001306130.2:c.4415_4417del