Canonical Allele Identifier: PA2826910970
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045744
ClinVar RCV Id: RCV002908868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Gln1041Lys
CA2094796
NM_001306129.2:c.3121C>A