Canonical Allele Identifier: PA2828176935
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352451.1:p.Tyr240Asp
CA350474250
NM_001365522.2:c.718T>G