Allele Registry

Canonical Allele Identifier: PA2829854910

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV001663503

RCV001825013

ClinVar Variation:

1256161

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Ser247Ile	CA399983393 NM_016834.5:c.740G>T