Canonical Allele Identifier: PA2826912178
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16324
ClinVar RCV Id: RCV000017721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Leu1884Arg
CA126366
NM_001306130.2:c.5651T>G