Allele Registry

Canonical Allele Identifier: PA2826264804

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Lys257Thr	CA225413 NM_001203252.2:c.770A>C