Allele Registry

Canonical Allele Identifier: PA2826264844

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Lys338Ile	CA225492 NM_001203252.2:c.1013A>T