Allele Registry

Canonical Allele Identifier: PA100490

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Lys574Thr	CA225413 NM_016835.5:c.1721A>C