Allele Registry

Canonical Allele Identifier: PA225414

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015328

RCV000084515

ClinVar Variation:

14259

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Lys257Thr	CA225413 NM_005910.6:c.770A>C