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
ENSP00000408975.3:p.Asn238del
ENST00000446361.7:c.713_715del
ENST00000446361.7:c.[713_715del;717C>A]
ENST00000446361.7:c.[713_715del;717C>T]
