Allele Registry

Canonical Allele Identifier: PA2573074211

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084507

RCV000246568

RCV001514001

ClinVar Variation:

98202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Tyr516His	CA225397 NM_001377265.1:c.1546T>C