Allele Registry

Canonical Allele Identifier: PA2499255663

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV001663503

RCV001825013

ClinVar Variation:

1256161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Ser697Ile	CA399983393 NM_001377265.1:c.2090G>T