Allele Registry

Canonical Allele Identifier: PA645447415

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000356485

RCV000532567

RCV001531268

RCV004526663

ClinVar Variation:

323645

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Ala469Thr	CA8617962 NM_016835.5:c.1405G>A