Allele Registry

Canonical Allele Identifier: PA915977237

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015336

RCV000084517

ClinVar Variation:

14266

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Leu601Val	CA225417 NM_001123066.4:c.1801C>G