Allele Registry

Canonical Allele Identifier: PA2826911856

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000190733

ClinVar Variation:

208716

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293059.2:p.Trp1017Cys	CA204749 NM_001306130.2:c.3051G>T CA350489456 NM_001306130.2:c.3051G>C