Allele Registry

Canonical Allele Identifier: PA2573074245

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084551

RCV000692998

RCV003905079

ClinVar Variation:

98231

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Val755Ile	CA225490 NM_001377265.1:c.2263G>A