Canonical Allele Identifier: PA2826913790
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2238487
ClinVar RCV Id: RCV002729256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293061.2:p.Ile1791Phe
CA350470888
NM_001306132.2:c.5371A>T