Allele Registry

Canonical Allele Identifier: PA2825588864

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015331

RCV000084544

RCV000995804

ClinVar Variation:

14262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Ser291Phe	CA225475 NM_001123067.4:c.872C>T