ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139676620
Gene: MAPT
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001116538.2:p.Asn631del
NM_001123066.4:c.1892_1894del
NM_001123066.4:c.[1892_1894del;1896C>A]
NM_001123066.4:c.[1892_1894del;1896C>T]