Canonical Allele Identifier: PA2828176664
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16324
ClinVar RCV Id: RCV000017721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Leu1884Arg
CA126366
NM_001365521.2:c.5651T>G