Allele Registry

Canonical Allele Identifier: PA915977292

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Val672Met	CA225483 NM_001123066.4:c.2014G>A