Canonical Allele Identifier: PA2826912952
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16323
ClinVar RCV Id: RCV000017720
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Trp1744Arg
CA126364
NM_001306131.2:c.5230T>A
CA350471586
NM_001306131.2:c.5230T>C