Allele Registry

Canonical Allele Identifier: PA2826264626

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015331

RCV000084544

RCV000995804

ClinVar Variation:

14262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Ser260Phe	CA225475 NM_001203251.2:c.779C>T