Allele Registry

Canonical Allele Identifier: PA225493

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Lys369Ile	CA225492 NM_005910.6:c.1106A>T