Canonical Allele Identifier: PA2828169621
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536417
ClinVar RCV Id: RCV003266301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352446.1:p.Thr1843Ser
CA350471472
NM_001365517.2:c.5528C>G
CA350471484
NM_001365517.2:c.5527A>T