Canonical Allele Identifier: PA2828175611
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Cys123Arg
CA350478685
NM_001365521.2:c.367T>C