Allele Registry

Canonical Allele Identifier: PA2826264679

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015330

RCV000266864

ClinVar Variation:

14261

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Arg5His	CA257191 NM_001203252.2:c.14G>A