Allele Registry

Canonical Allele Identifier: PA2828704039

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364197.1:p.Glu253Val	CA225485 NM_001377268.1:c.758A>T