Canonical Allele Identifier: PA2828170310
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352447.1:p.Cys258Tyr
CA350473836
NM_001365518.2:c.773G>A