Allele Registry

Canonical Allele Identifier: PA2825588897

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015316

RCV000084554

RCV002476970

ClinVar Variation:

14247

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Arg377Trp	CA225495 NM_001123067.4:c.1129C>T