Canonical Allele Identifier: PA2828172269
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424646
ClinVar RCV Id: RCV000509587 RCV000570760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352448.1:p.Tyr240Asp
CA350474250
NM_001365519.2:c.718T>G