Allele Registry

Canonical Allele Identifier: PA225398

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084507

RCV000246568

RCV001514001

ClinVar Variation:

98202

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Tyr441His	CA225397 NM_016835.5:c.1321T>C