Canonical Allele Identifier: PA2828175710
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Cys258Tyr
CA350473836
NM_001365521.2:c.773G>A