Allele Registry

Canonical Allele Identifier: PA2825588673

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV001663503

RCV001825013

ClinVar Variation:

1256161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Ser640Ile	CA399983393 NM_001123066.4:c.1919G>T