Allele Registry

Canonical Allele Identifier: PA100515

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015313

RCV000084527

RCV000763405

RCV002508757

RCV003407335

ClinVar Variation:

14245

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Pro618Leu	CA225444 NM_016835.5:c.1853C>T