Canonical Allele Identifier: PA2826912416
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Tyr240Asp
CA350474250
NM_001306131.2:c.718T>G