Allele Registry

Canonical Allele Identifier: PA2825588870

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Val308Met	CA225483 NM_001123067.4:c.922G>A