Allele Registry

Canonical Allele Identifier: PA2826264632

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Val277Met	CA225483 NM_001203251.2:c.829G>A