Canonical Allele Identifier: PA2828169161
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2380311
ClinVar RCV Id: RCV002688919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Ile1069Leu
CA2094772
NM_001365517.2:c.3205A>T
CA350489129
NM_001365517.2:c.3205A>C