Canonical Allele Identifier: PA2826910636
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424644
ClinVar RCV Id: RCV000509582 RCV000575065 RCV002526994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293058.2:p.Cys123Arg
CA350478685
NM_001306129.2:c.367T>C