Allele Registry

Canonical Allele Identifier: PA2829347362

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000190733

ClinVar Variation:

208716

HGVS (amino-acid)	Matching Registered Transcripts
NP_002017.2:p.Trp1017Cys	CA204749 NM_002026.4:c.3051G>T CA350489456 NM_002026.4:c.3051G>C