Allele Registry

Canonical Allele Identifier: PA2829854835

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Lys199Thr	CA225413 NM_016834.5:c.596A>C