Allele Registry

Canonical Allele Identifier: PA225489

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Ser669Leu	CA225487 NM_016835.5:c.2006C>T