Allele Registry

Canonical Allele Identifier: PA225426

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015322

RCV000084521

RCV000763404

ClinVar Variation:

14253

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Asn250Lys	CA225424 NM_001123067.4:c.750T>G CA399983169 NM_001123067.4:c.750T>A