Allele Registry

Canonical Allele Identifier: PA2573074240

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Val729Met	CA225483 NM_001377265.1:c.2185G>A