Canonical Allele Identifier: PA2826911859
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492983
ClinVar RCV Id: RCV001984020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Arg1028Gln
CA350489398
NM_001306130.2:c.3083G>A