Allele Registry

Canonical Allele Identifier: PA2829854935

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Val279Met	CA225483 NM_016834.5:c.835G>A