Allele Registry

Canonical Allele Identifier: PA2826264633

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Glu282Val	CA225485 NM_001203251.2:c.845A>T