Canonical Allele Identifier: PA2828170313
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352447.1:p.Cys260Gly
CA350473823
NM_001365518.2:c.778T>G