Allele Registry

Canonical Allele Identifier: PA2825588855

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Gly274Val	CA225451 NM_001123067.4:c.821G>T