Allele Registry

Canonical Allele Identifier: PA225486

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Glu342Val	CA225485 NM_005910.6:c.1025A>T