Canonical Allele Identifier: PA2828176647
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16323
ClinVar RCV Id: RCV000017720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352450.1:p.Trp1835Arg
CA126364
NM_001365521.2:c.5503T>A
CA350471586
NM_001365521.2:c.5503T>C