Canonical Allele Identifier: PA2826911869
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1495273
ClinVar RCV Id: RCV001991299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293059.2:p.Val1048Ala
CA350489280
NM_001306130.2:c.3143T>C