Allele Registry

Canonical Allele Identifier: PA2829855725

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_058525.1:p.Glu253Val	CA225485 NM_016841.5:c.758A>T