Canonical Allele Identifier: PA2826911887
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2961093
ClinVar RCV Id: RCV003819804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Glu1074Gly
CA350489059
NM_001306130.2:c.3221A>G