Allele Registry

Canonical Allele Identifier: PA2825588871

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Glu313Val	CA225485 NM_001123067.4:c.938A>T