Allele Registry

Canonical Allele Identifier: PA2825588885

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Lys340Ile	CA225492 NM_001123067.4:c.1019A>T