Allele Registry

Canonical Allele Identifier: PA2829854907

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Gly245Val	CA225451 NM_016834.5:c.734G>T