Allele Registry

Canonical Allele Identifier: PA915977231

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Lys592Thr	CA225413 NM_001123066.4:c.1775A>C