Allele Registry

Canonical Allele Identifier: PA2826264625

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015338

RCV000084543

ClinVar Variation:

14268

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Lys257Met	CA225473 NM_001203251.2:c.770A>T