Allele Registry

Canonical Allele Identifier: PA2573074241

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Glu734Val	CA225485 NM_001377265.1:c.2201A>T