Allele Registry

Canonical Allele Identifier: PA225484

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015321

RCV000084548

ClinVar Variation:

14252

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Val337Met	CA225483 NM_005910.6:c.1009G>A