Canonical Allele Identifier: PA2826910697
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Cys260Gly
CA350473823
NM_001306129.2:c.778T>G