Allele Registry

Canonical Allele Identifier: PA2826264659

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015316

RCV000084554

RCV002476970

ClinVar Variation:

14247

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Arg346Trp	CA225495 NM_001203251.2:c.1036C>T