Canonical Allele Identifier: PA2828171626
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 192244
ClinVar RCV Id: RCV000207361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352447.1:p.Trp1834Cys
CA352250
NM_001365518.2:c.5502G>C
CA350471577
NM_001365518.2:c.5502G>T