Allele Registry

Canonical Allele Identifier: PA2826264647

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Lys309Ile	CA225492 NM_001203251.2:c.926A>T