Allele Registry

Canonical Allele Identifier: PA225418

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015336

RCV000084517

ClinVar Variation:

14266

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Leu266Val	CA225417 NM_005910.6:c.796C>G