ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916039417
Gene: F11
HGNC
NCBI
Linked Data
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Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001341733.1:p.Ala43Thr
NM_001354804.2:c.127G>A