Canonical Allele Identifier: PA2826912969
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 192245
ClinVar RCV Id: RCV000207403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Leu1793Pro
CA352252
NM_001306131.2:c.5378T>C