Canonical Allele Identifier: PA2828171636
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_001352447.1:p.Thr1842Ser
CA350471472
NM_001365518.2:c.5525C>G
CA350471484
NM_001365518.2:c.5524A>T