Allele Registry

Canonical Allele Identifier: PA100463

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Gly620Val	CA225451 NM_016835.5:c.1859G>T