Allele Registry

Canonical Allele Identifier: PA2826264607

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Lys228Thr	CA225413 NM_001203251.2:c.683A>C