Allele Registry

Canonical Allele Identifier: PA225452

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Gly303Val	CA225451 NM_005910.6:c.908G>T