Allele Registry

Canonical Allele Identifier: PA2573074243

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Ser744Leu	CA225487 NM_001377265.1:c.2231C>T