Canonical Allele Identifier: PA2828169620
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444867
ClinVar RCV Id: RCV001982630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Thr1841Met
CA2094033
NM_001365517.2:c.5522C>T