Canonical Allele Identifier: PA2573102274
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16323
ClinVar RCV Id: RCV000017720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997647.2:p.Trp1925Arg
CA126364
NM_212482.4:c.5773T>A
CA350471586
NM_212482.4:c.5773T>C