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
XP_005257427.1:p.Asn333del
XM_005257370.4:c.998_1000del
XM_005257370.4:c.[998_1000del;1002C>A]
XM_005257370.4:c.[998_1000del;1002C>T]
