Canonical Allele Identifier: PA2826911306
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16324
ClinVar RCV Id: RCV000017721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Leu1974Arg
CA126366
NM_001306129.2:c.5921T>G