Allele Registry

Canonical Allele Identifier: PA2826264823

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015331

RCV000084544

RCV000995804

ClinVar Variation:

14262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Ser289Phe	CA225475 NM_001203252.2:c.866C>T