ClinGen Allele Registry
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This allele is not present in the registry. To get a canonical identifier, please click on the "Get identifier" below.
Canonical Allele Identifier:
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Gene: F11
HGNC
NCBI
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
ENSP00000264692.5:p.Ile161_Asp162del
ENST00000264692.8:c.482_487del
ENST00000264692.8:c.[482_487del;489T>C]
