Allele Registry

Canonical Allele Identifier: PA2829855423

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV001663503

RCV001825013

ClinVar Variation:

1256161

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Ser622Ile	CA399983393 NM_016835.5:c.1865G>T