Allele Registry

Canonical Allele Identifier: PA2828703707

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364195.1:p.Lys583Thr	CA225413 NM_001377266.1:c.1748A>C