Canonical Allele Identifier: PA199118
Gene: F11 HGNC NCBI

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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000119.1:p.Gln244Ter
NM_000128.4:c.[729_735del;737G>T;739C>A]

NM_000128.4:c.730C>T