Allele Registry

Canonical Allele Identifier: PA2826264830

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Glu311Val	CA225485 NM_001203252.2:c.932A>T