Allele Registry

Canonical Allele Identifier: PA100445

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Glu659Val	CA225485 NM_016835.5:c.1976A>T