Allele Registry

Canonical Allele Identifier: PA915977293

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Glu677Val	CA225485 NM_001123066.4:c.2030A>T