Allele Registry

Canonical Allele Identifier: PA100456

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015315

RCV000084519

ClinVar Variation:

14246

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Gly589Val	CA225421 NM_016835.5:c.1766G>T