Canonical Allele Identifier: PA2826912367
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Cys123Arg
CA350478685
NM_001306131.2:c.367T>C