Canonical Allele Identifier: PA2828169156
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1670543
ClinVar RCV Id: RCV002203834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Val1064Ile
CA2094775
NM_001365517.2:c.3190G>A