Canonical Allele Identifier: PA2829346785
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002017.2:p.Cys258Tyr
CA350473836
NM_002026.4:c.773G>A