Allele Registry

Canonical Allele Identifier: PA2825588828

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Lys228Thr	CA225413 NM_001123067.4:c.683A>C