Allele Registry

Canonical Allele Identifier: PA2828703732

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364195.1:p.Val632Met	CA225483 NM_001377266.1:c.1894G>A