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: MAPT
HGNC
NCBI
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_005901.2:p.Asn296del
NM_005910.6:c.887_889del
NM_005910.6:c.[887_889del;891C>A]
NM_005910.6:c.[887_889del;891C>T]
