Allele Registry

Canonical Allele Identifier: PA2825588590

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084507

RCV000246568

RCV001514001

ClinVar Variation:

98202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Tyr441His	CA225397 NM_001123066.4:c.1321T>C