Canonical Allele Identifier: PA2826910695
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Cys258Tyr
CA350473836
NM_001306129.2:c.773G>A