Canonical Allele Identifier: PA2826911880
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1670543
ClinVar RCV Id: RCV002203834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Val1064Ile
CA2094775
NM_001306130.2:c.3190G>A