Allele Registry

Canonical Allele Identifier: PA2573074247

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Lys761Ile	CA225492 NM_001377265.1:c.2282A>T