Allele Registry

Canonical Allele Identifier: PA915977318

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Lys704Ile	CA225492 NM_001123066.4:c.2111A>T