Canonical Allele Identifier: PA1139676620
Gene: MAPT HGNC NCBI

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]